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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633279Generated: November 1, 2026

2-((tert-Butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoic acid → 1-(6-Benzoylamino-9H-purin-9-yl)-3-[N-tert-butoxycarbonyl-beta-(4-fluorophenyl)-D,L-alanylamino]-1,3-dideoxy-beta-D-ribofuranuronic acid

https://huagongshe.com/reaction/1633279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((tert-Butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoic acidHCID 2756794—
Reactant3-amino-1-(6-benzoylamino-9H-purin-9-yl)-1,3-dideoxy-beta-D-ribofuranuronic acidHCID 53854008—
Product1-(6-Benzoylamino-9H-purin-9-yl)-3-[N-tert-butoxycarbonyl-beta-(4-fluorophenyl)-D,L-alanylamino]-1,3-dideoxy-beta-D-ribofuranuronic acidHCID 2282822688.6%

Reaction Steps

1-(6-Benzoylamino-9H-purin-9-yl)-3-[N-tert-butoxycarbonyl-β-(4-fluorophenyl)-D,L-alanylamino]-1,3-dideoxy-β-D-ribofuranuronic acid (575 mg) was prepared by reacting 1-(6-benzoylamino-9H-purin-9-yl)-1,3-dideoxy-3-amino-β-D-ribofuranuronic acid (384 mg) prepared in Example 1 with N-hydroxysuccinimide ester of N-tert-butoxycarbonyl-β-(4-fluorophenyl)-D,L-alanine (417 mg) according to a similar manner to that of Example 5, mp. 125°-134° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04479942
Source datasetuspto-grants-1984_10
ORD IDord-a4be331eb3924bcaa1d9aae245211d14
Source noteuspto-grants-1984_10